All diseases

2 entries on 1 page. Showing entries 1 - 2.
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ID     

AscendingAbbreviation     

Name     

OMIM ID     

Inheritance     

Individuals     

Phenotypes     

Associated with genes

Associated tissues

Disease features
04451 MRD33 mental retardation, autosomal dominant, type 33 (MRD-33) 616311 - - - DPP6 - -
00295 VF2 fibrillation, ventricular, paroxysmal, familial, type 2 (VF-2) 612956 AD 1 1 DPP6 - -
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